Evidence map›Paper›PMID 31467080›Full record

ArticleThe Journal of biological chemistry2019

Design and development of stapled transmembrane peptides that disrupt the activity of G-protein-coupled receptor oligomers.

Joaquín Botta, Lucka Bibic, Patrick Killoran, Peter J McCormick, Lesley A Howell

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 32 citations in OpenAlex.

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  8. An extended conformation of SARS-CoV-2 main protease reveals allosteric targets.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
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  12. Probing GPCR Dimerization Using Peptides.Frontiers in endocrinology · 2022
    Review
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  14. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Joaquín BottaCentre for Endocrinology, William Harvey Research Institute, Bart's and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, United Kingdom.
Lucka BibicSchool of Pharmacy, University of East Anglia, Norwich Research Park, Norwich NR4 7TJ, United Kingdom.
Patrick KilloranSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, United Kingdom.
Peter J McCormickCentre for Endocrinology, William Harvey Research Institute, Bart's and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, United Kingdom p.mccormick@qmul.ac.uk.ORCID 0000-0002-2225-5181
Lesley A HowellSchool of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London E1 4NS, United Kingdom l.howell@qmul.ac.uk.
William Harvey Research Institute · GBLiverpool John Moores University · GBNorwich Research Park · GBQueen Mary University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane proteins can associate into larger complexes. Examples include receptor tyrosine complexes, ion channels, transporters, and G protein-coupled receptors (GPCRs). For the latter, there is abundant evidence indicating that GPCRs assemble into complexes, through both homo- and heterodimerization. However, the tools for studying and disrupting these complexes, GPCR or otherwise, are limited. Here, we have developed stabilized interference peptides for this purpose. We have previously reported that tetrahydrocannabinol-mediated cognitive impairment arises from homo- or heterooligomerization between the GPCRs cannabinoid receptor type 1 (CB

Indexed as

Amino Acid SequenceCalciumCyclic AMPDimerizationHEK293 CellsHumansNanotechnologyPeptidesProtein Interaction Domains and MotifsReceptor, Cannabinoid, CB1Receptor, Serotonin, 5-HT2AReceptors, G-Protein-CoupledCalciumCyclic AMPPeptidesReceptor, Cannabinoid, CB1Receptor, Serotonin, 5-HT2AReceptors, G-Protein-Coupledbimolecular fluorescence complementationcannabinoid receptor type 1 (CB1)cell-penetrating peptide (CPP)dimerizationG protein-coupled receptor (GPCR)hydrocarbon staplingNanoLuc binary technology (NanoBiT)peptide chemical synthesisprotein-protein interactionserotonin receptor type 2A (5HT2A)transmembrane peptide

Identifiers

PMID31467080
PMCPMC6851324
OpenAlexW2970240009

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.